Canonical Allele Identifier: CA359394182
Gene: SLC45A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33963942T>A , CM000667.2:g.33963942T>A GRCh38
NC_000005.9:g.33964047T>A , CM000667.1:g.33964047T>A GRCh37
NC_000005.8:g.33999804T>A NCBI36
NG_011691.2:g.25734A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.637A>T MANE Select ENSP00000296589.4:p.Thr213Ser
ENST00000296589.8:c.637A>T ENSP00000296589.4:p.Thr213Ser
ENST00000382102.7:c.637A>T ENSP00000371534.3:p.Thr213Ser
ENST00000505056.1:n.439A>T
ENST00000509381.1:c.563-9438A>T ENSP00000421100.1:n.563-9438A>T
ENST00000510600.1:c.112A>T ENSP00000424010.1:p.Thr38Ser
NM_001012509.3:c.637A>T NP_001012527.1:p.Thr213Ser
NM_001297417.2:c.563-9438A>T NP_001284346.2:n.563-9438A>T
NM_016180.4:c.637A>T NP_057264.3:p.Thr213Ser
XM_011514051.1:c.235A>T XP_011512353.1:p.Thr79Ser
XM_011514052.1:c.637A>T XP_011512354.1:p.Thr213Ser
XR_925620.1:n.1454A>T
NM_016180.5:c.637A>T MANE Select NP_057264.4:p.Thr213Ser
NM_001012509.4:c.637A>T NP_001012527.2:p.Thr213Ser
NM_001297417.3:c.563-9438A>T NP_001284346.2:n.563-9438A>T
NM_001297417.4:c.563-9438A>T NP_001284346.2:n.563-9438A>T